Experteer Overview
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In this role you will provide medical leadership for clinical trials, acting as the internal medical expert and guiding study design, safety management, and reporting. You will collaborate across departments to support feasibility, design, educational efforts, and medical communications, while contributing to business development through sponsor interactions. The position offers hybrid work options after training and places a strong emphasis on scientific excellence and patient outcomes. You will help shape trial strategy and ensure regulatory compliance within a dynamic, cross-functional team.
Compensaciones / Incentivos
• Provide medical management and expertise for clinical trials
• Contribute medical input to study reports, regulatory documents, and manuscripts
• Manage safety issues in clinical trials with cross-functional evaluation




• Participate in new business development through proposal and sponsor meetings
• Coordinate with other departments across all study phases (feasibility, design, medical information, documentation)
• Lead adherence to research-related protocols and policies
• Develop new clinical projects including study design, protocols, and project plans
Responsabilidades
• MD or equivalent
• xqbhyrx Board certification and current medical licensure preferred
• Prior clinical trial research experience preferred
• Previous experience in pharmaceutical-related clinical research preferred
Requisitos principales
• competitive compensation
• health and wellness benefits
• retirement benefits
• paid time off (PTO)
• office-based culture with hybrid WFH after training
• company-sponsored social events

📌 Hepatology - Medical Director (Madrid)
🏢 Medpace
📍 Madrid